SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions
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Browse genes associated with cancer risk that contain miRNA related somatic mutations

Somatic mutations that alter miRNA target sites: CLASH [8 records found]

[download data table]

Transcript ID	Gene Symbol	Mutation ID
NM_001278210	NUP153	chr6:g.17629108T>G
NM_001278210	NUP153	chr6:g.17629110A>G
NM_001278210	NUP153	chr6:g.17629126G>A
NM_001278210	NUP153	chr6:g.17629140C>A
NM_001278210	NUP153	chr6:g.17637481G>T
NM_001278210	NUP153	chr6:g.17637601A>C
NM_001278210	NUP153	chr6:g.17637605A>T
NM_001278210	NUP153	chr6:g.17637627T>C

Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [106 records found]

[download data table]

Transcript ID	Gene Symbol	Mutation ID
hsa_circ_0075703	NUP153	chr6:g.17615745G>A
hsa_circ_0075703	NUP153	chr6:g.17616025G>A
hsa_circ_0075725	NUP153	chr6:g.17654855T>G
NM_001278210	NUP153	chr6:g.17706392C>A
hsa_circ_0075704	NUP153	chr6:g.17616633G>A
hsa_circ_0075704	NUP153	chr6:g.17616654T>A
hsa_circ_0075707	NUP153	chr6:g.17624570C>T
hsa_circ_0075707	NUP153	chr6:g.17624697T>G
hsa_circ_0075707	NUP153	chr6:g.17624701C>T
hsa_circ_0075707	NUP153	chr6:g.17624707C>G
hsa_circ_0075708	NUP153	chr6:g.17625813C>G
hsa_circ_0075708	NUP153	chr6:g.17625916A>T
hsa_circ_0075708	NUP153	chr6:g.17625986T>C
hsa_circ_0075708	NUP153	chr6:g.17626003A>G
hsa_circ_0075708	NUP153	chr6:g.17626016C>T
hsa_circ_0075708	NUP153	chr6:g.17628693C>T
hsa_circ_0075708	NUP153	chr6:g.17628772G>T
hsa_circ_0075708	NUP153	chr6:g.17628782G>A
hsa_circ_0075708	NUP153	chr6:g.17628821G>T
hsa_circ_0075708	NUP153	chr6:g.17628834C>T
hsa_circ_0075708	NUP153	chr6:g.17628849T>A
hsa_circ_0075708	NUP153	chr6:g.17628853CCC>TTC
hsa_circ_0075708	NUP153	chr6:g.17628875A>G
hsa_circ_0075708	NUP153	chr6:g.17628924T>A
hsa_circ_0075708	NUP153	chr6:g.17629011T>C
hsa_circ_0075708	NUP153	chr6:g.17629022A>G
hsa_circ_0075708	NUP153	chr6:g.17629022A>C
hsa_circ_0075708	NUP153	chr6:g.17629042A>T
hsa_circ_0075708	NUP153	chr6:g.17629108T>G
hsa_circ_0075708	NUP153	chr6:g.17629110A>G
hsa_circ_0075708	NUP153	chr6:g.17629126G>A
hsa_circ_0075708	NUP153	chr6:g.17629140C>A
hsa_circ_0075708	NUP153	chr6:g.17629458C>T
hsa_circ_0075708	NUP153	chr6:g.17629514G>A
hsa_circ_0075711	NUP153	chr6:g.17632694T>C
hsa_circ_0075711	NUP153	chr6:g.17632826C>T
hsa_circ_0075711	NUP153	chr6:g.17632830G>A
hsa_circ_0075719	NUP153	chr6:g.17637225G>T
hsa_circ_0075719	NUP153	chr6:g.17637230C>A
hsa_circ_0075719	NUP153	chr6:g.17637247C>G
hsa_circ_0075719	NUP153	chr6:g.17637290G>T
hsa_circ_0075719	NUP153	chr6:g.17637306A>T
hsa_circ_0075719	NUP153	chr6:g.17637315G>C
hsa_circ_0075719	NUP153	chr6:g.17637319T>C
hsa_circ_0075719	NUP153	chr6:g.17637326C>T
hsa_circ_0075719	NUP153	chr6:g.17637346C>T
hsa_circ_0075719	NUP153	chr6:g.17637351C>T
hsa_circ_0075719	NUP153	chr6:g.17637373G>A
hsa_circ_0075719	NUP153	chr6:g.17637375C>T
hsa_circ_0075719	NUP153	chr6:g.17637420G>C
hsa_circ_0075719	NUP153	chr6:g.17637444A>G
hsa_circ_0075719	NUP153	chr6:g.17637481G>T
hsa_circ_0075719	NUP153	chr6:g.17637515A>G
hsa_circ_0075719	NUP153	chr6:g.17637517A>G
hsa_circ_0075719	NUP153	chr6:g.17637532T>A
hsa_circ_0075719	NUP153	chr6:g.17637533C>G
hsa_circ_0075719	NUP153	chr6:g.17637534A>G
hsa_circ_0075719	NUP153	chr6:g.17637535G>T
hsa_circ_0075719	NUP153	chr6:g.17637545C>T
hsa_circ_0075719	NUP153	chr6:g.17637601A>C
hsa_circ_0075719	NUP153	chr6:g.17637605A>T
hsa_circ_0075719	NUP153	chr6:g.17637627T>C
hsa_circ_0075719	NUP153	chr6:g.17637726G>A
hsa_circ_0075720	NUP153	chr6:g.17640020C>T
hsa_circ_0075720	NUP153	chr6:g.17640044A>G
hsa_circ_0075725	NUP153	chr6:g.17647819A>G
hsa_circ_0075725	NUP153	chr6:g.17647835C>T
hsa_circ_0075725	NUP153	chr6:g.17647838C>A
hsa_circ_0075725	NUP153	chr6:g.17647850C>T
hsa_circ_0075725	NUP153	chr6:g.17647859T>G
hsa_circ_0075725	NUP153	chr6:g.17647872C>T
hsa_circ_0075725	NUP153	chr6:g.17649226T>C
hsa_circ_0075725	NUP153	chr6:g.17649259C>T
hsa_circ_0075731	NUP153	chr6:g.17662047A>G
hsa_circ_0075735	NUP153	chr6:g.17665315G>T
hsa_circ_0075735	NUP153	chr6:g.17665318G>A
hsa_circ_0075735	NUP153	chr6:g.17665325A>G
hsa_circ_0075739	NUP153	chr6:g.17669482C>A
hsa_circ_0075739	NUP153	chr6:g.17669502A>G
hsa_circ_0075739	NUP153	chr6:g.17669505A>T
hsa_circ_0075739	NUP153	chr6:g.17669526G>T
hsa_circ_0075741	NUP153	chr6:g.17674952G>A
hsa_circ_0075741	NUP153	chr6:g.17674959C>T
hsa_circ_0075741	NUP153	chr6:g.17674976C>A
hsa_circ_0075741	NUP153	chr6:g.17674978TA>A
hsa_circ_0075741	NUP153	chr6:g.17674985C>T
hsa_circ_0075741	NUP153	chr6:g.17675242G>T
hsa_circ_0075741	NUP153	chr6:g.17675247C>T
hsa_circ_0075741	NUP153	chr6:g.17675261T>C
hsa_circ_0075741	NUP153	chr6:g.17675333C>G
hsa_circ_0075741	NUP153	chr6:g.17675344C>T
hsa_circ_0075741	NUP153	chr6:g.17675578A>G
hsa_circ_0075741	NUP153	chr6:g.17675614C>T
hsa_circ_0075741	NUP153	chr6:g.17675623C>T
hsa_circ_0075741	NUP153	chr6:g.17675643G>A
hsa_circ_0075741	NUP153	chr6:g.17675643G>T
hsa_circ_0075741	NUP153	chr6:g.17675646C>G
hsa_circ_0075741	NUP153	chr6:g.17675708C>T
hsa_circ_0075741	NUP153	chr6:g.17675750G>A
hsa_circ_0075741	NUP153	chr6:g.17675759A>G
hsa_circ_0075741	NUP153	chr6:g.17688438G>A
hsa_circ_0075741	NUP153	chr6:g.17688477C>T
hsa_circ_0075741	NUP153	chr6:g.17688510G>A
hsa_circ_0075741	NUP153	chr6:g.17688512G>A
NM_001278210	NUP153	chr6:g.17706357G>T
NM_001278210	NUP153	chr6:g.17706377G>A

Somatic mutations that alter predicted mRNA-miRNA target sites [3 records found]

[download data table]

Transcript ID	Gene Symbol	Mutation ID
NM_005124	NUP153	chr6:g.17616025G>A
NM_005124	NUP153	chr6:g.17615745G>A
NM_005124	NUP153	chr6:g.17615272T>A